ClinConnect ClinConnect Logo
Search / Trial NCT06465810

Non-interventional Study of Patients With Transthyretin (ATTR) Amyloidosis

Launched by ASTRAZENECA · Jun 13, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Amyloidosis Transthyretin Hereditary Transthyretin Mediated (H Attr) Amyloidosis H Attr Amyloidosis Hereditary Attr Amyloidosis Wild Type Amyloidosis Wt Attr Amyloidosis Att Rv Amyloidosis Att Rwt Amyloidosis Polyneuropathy Familial Amyloid Polyneuropathies Attr Transthyretin Amyloidosis Ttr Mediated Amyloidosis Polyneuropathies Amyloid Neuropathies Amyloid Neuropathies, Familial Amyloidosis, Familial Eplontersen Non Interventional Observational Real World

ClinConnect Summary

The MaesTTRo study is looking at patients with transthyretin amyloidosis (ATTR), a condition where abnormal proteins build up in the body, affecting various organs. This research aims to understand how the disease progresses over time and to gather information about the treatments patients are using in the real world. One of the treatments being studied is called eplontersen, which helps reduce the harmful proteins in the body. The study is currently recruiting participants aged 18 and older who have a confirmed diagnosis of ATTR amyloidosis and are willing to share their health experiences.

If you decide to participate, you will be asked to provide consent and participate in tracking your health outcomes through questionnaires. However, you will not be eligible if you're already part of another clinical trial for ATTR amyloidosis or if you have certain other types of amyloidosis. This study is an important step in learning more about ATTR and helping improve treatment options for patients in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patient willing and able to provide written informed consent to participate in the study
  • Confirmed diagnosis of amyloid transthyretin (ATTR) amyloidosis
  • Aged ≥18 years at the time of signing the informed consent
  • Patient willing and able to participate in collection of electronic patient reported outcomes (PROs)
  • Exclusion Criteria:
  • Concurrent participation in any interventional trial for ATTR amyloidosis
  • Involvement in the planning and/or conduct of the current study
  • Patients with evidence of primary or light chain amyloidosis (AL) or serum protein A amyloidosis (AA)
  • Asymptomatic patients with ATTR amyloidosis and asymptomatic ATTR mutation carriers

About Astrazeneca

AstraZeneca is a global biopharmaceutical company dedicated to the discovery, development, and commercialization of innovative medicines across various therapeutic areas, including oncology, cardiovascular, respiratory, and autoimmune diseases. With a strong commitment to scientific research and patient-centric solutions, AstraZeneca leverages cutting-edge technology and a robust pipeline to address unmet medical needs. The company collaborates with healthcare professionals, academic institutions, and other organizations to advance clinical trials and deliver transformative therapies, aiming to improve health outcomes and enhance the quality of life for patients worldwide.

Locations

Los Angeles, California, United States

Durham, North Carolina, United States

Dallas, Texas, United States

Berlin, , Germany

Philadelphia, Pennsylvania, United States

New Haven, Connecticut, United States

La Jolla, California, United States

Washington, District Of Columbia, United States

Kansas City, Missouri, United States

Saint Louis, Missouri, United States

New York, New York, United States

Germantown, Tennessee, United States

London, Ontario, Canada

Glasgow, , United Kingdom

Richmond, Virginia, United States

Greenville, South Carolina, United States

Boston, Massachusetts, United States

Milwaukee, Wisconsin, United States

New Brunswick, New Jersey, United States

Manhasset, New York, United States

Vancouver, British Columbia, Canada

Vancouver, British Columbia, Canada

London, , United Kingdom

Homburg, Saarland, Germany

New York, New York, United States

Nashville, Tennessee, United States

Hannover, Lower Saxony, Germany

Toronto, Ontario, Canada

Seattle, Washington, United States

Halifax, Nova Scotia, Canada

San Francisco, California, United States

Indianapolis, Indiana, United States

Frankfurt, Essen, Germany

Mainz, Rhineland Palatinate, Germany

Aachen, Nrw, Germany

Wuerzburg, Bavaria, Germany

San Francisco, California, United States

Nashville, Tennessee, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported